Aktualnie prowadzone rekrutacje

With offices in Berlin, Warsaw and Prague, KCR Placement is an international boutique provider of ‘fit for purpose’ resourcing solutions for a wide array of functions, including expert, managerial and senior executive ones. We specialize in finding the right talents for Pharmaceutical, Biotech, Medical Device companies and Contract Research Organizations across Europe. 

We're onboarding best-in-class candidates, so give us a chance to meet you!

Current Vacancy Highlights:

Freelance Clinical Research Associate / Moldova
International, rapidly growing CRO is seeking a talented Freelancer Clinical Research Associate The new incumbent will be accountable for study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files. CRA also ensures the quality and integrity of data, compliance with relevant SOPs and regulatory requirements and study completion on time and within budget.
Our Clients are a full service globally based Contract Research Organisation with in-depth experience of the most challenging therapeutic areas. They are seeking an experienced Clinical Research Associate, to come on board to assist with the monitoring of their growing portfolio of projects. 
We are currently hiring for Freelance CRA (all seniority levels), a variety of Sponsors who are Top 10 Pharmaceutical Companies. Interesting studies, possibilities to adjust to your expectations as per clinical career development.
Providing your application will give you access to recent job openings.
Freelance Clinical Research Associate



Location: Moldova  
Type of Contract: Freelance
Seniority: Senior/Associate

Duties associated with the role: 

  • Review approved protocol and ensure qualification, initiation, monitoring and closeout visits for research sites are carried out in full compliance
  • Ensure overall integrity of study and adherence to guidelines, protocol and regulations
  • Complete monitoring reports and follow up letters, including providing the summaries of significant findings, deviations, deficiencies and recommended actions to secure compliance
  • Take an active role in the project team by providing feedback and suggestions for successful completion of the project
  • Coach and mentor less experienced CRAs to assist in their development and training

Desired Skills and Experience:

  • University degree in life sciences/pharmacy/biotechnology
  • At least 1 year of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines
  • Computer competency
  • Fluent command of English
  • Ability to complete tasks in an accurate and timely manner
  • This is a really exciting opportunity to join a team dedicated to supporting the development of ground-breaking drugs.
We’re onboarding “best in class” candidates, so give us a chance to meet you!


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